Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1365557 | Bioorganic & Medicinal Chemistry Letters | 2007 | 5 Pages |
Abstract
A series of compounds originally derived from thalidomide were synthesized and evaluated. The most potent compounds in this series, 5HPP-33 and compound 20, inhibited NF-κB activation in HeLa cells. Preliminary study indicated that the mechanism of inhibition of NF-κB activation is through inhibition of its translocation from the cytoplasm to the nucleus.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Esperanza J. Carcache de-Blanco, Bulbul Pandit, Zhigen Hu, Jiandong Shi, Andrew Lewis, Pui-Kai Li,